DUSP27 | Mutation | Missense | ENST00000271385.5 |
g.167095134C>T
|
c.766C>T
|
p.Arg256Cys
|
probably damaging
| SNU387 |
DUSP27 | Mutation | Missense | ENST00000271385.5 |
g.167096035T>C
|
c.1667T>C
|
p.Phe556Ser
|
probably damaging
| SNU387 |
DUSP27 | Mutation | Missense | ENST00000271385.5 |
g.167096794C>T
|
c.2426C>T
|
p.Ala809Val
|
benign
| Huh6 |
DUSP27 | Mutation | Missense | ENST00000271385.5 |
g.167096794C>T
|
c.2426C>T
|
p.Ala809Val
|
benign
| JHH2 |
DUSP27 | Mutation | Missense | ENST00000271385.5 |
g.167095864G>A
|
c.1496G>A
|
p.Ser499Asn
|
benign
| SNU368 |